Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 6
rs10501320
MADD ; MADD-AS1
0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 5
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 5
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 5
rs8067056
MAPT
0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5
rs62081501 0.925 0.080 18 37627749 intron variant G/A snv 6.2E-02 4
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 4
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 4
rs1057518806
HMBS
1.000 0.040 11 119093155 frameshift variant G/- del 4
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 4
rs4752856
MTCH2
1.000 0.040 11 47626490 intron variant G/A snv 0.28 4
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 3
rs1426371
LOC105369965 ; WSCD2
1.000 0.040 12 108236003 intron variant G/A snv 0.20 3
rs13262595
LOC107986983 ; TSNARE1
1.000 0.040 8 142235609 intron variant A/C;G snv 3
rs353547
TWF2
0.925 0.080 3 52234850 intron variant T/C snv 0.64 3
rs4684833 1.000 0.040 3 11990245 intergenic variant C/T snv 0.79 2
rs483143 0.925 0.080 6 27878966 intergenic variant G/C snv 0.13 2
rs80533 1.000 0.040 22 40689965 intergenic variant A/G snv 0.81 2
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 2
rs62064641
ARHGAP27
1.000 0.040 17 45411426 intron variant T/C snv 0.14 2
rs12765002
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102875591 intron variant C/T snv 0.24 2
rs56133711
BDNF
1.000 0.040 11 27701787 intron variant G/A snv 0.19 2
rs10507274
C12orf49
1.000 0.040 12 116723171 missense variant T/C snv 4.7E-02 4.4E-02 2
rs1248860
CADM2
1.000 0.040 3 84966628 intron variant G/A snv 0.56 2